| Identification | Back Directory | [Name]
tert-butyl 4-(mercaptomethyl)piperidine-1-carboxylate | [CAS]
581060-27-7 | [Synonyms]
1-Boc-4-(Mercaptomethyl) 1-Boc-4-(MercaptoMethyl)piperidine tert-butyl 4-(sulfanylmethyl)piperidine-1-carboxylate tert-butyl 4-(mercaptomethyl)piperidine-1-carboxylate 4-Mercaptomethyl-piperidine-1-carboxylic acid tert-butyl ester 4-(Mercaptomethyl)-1-piperidinecarboxylic acid tert-butyl ester 1-Piperidinecarboxylic acid, 4-(mercaptomethyl)-, 1,1-dimethylethyl ester | [Molecular Formula]
C11H21NO2S | [MOL File]
581060-27-7.mol | [Molecular Weight]
231.35 |
| Chemical Properties | Back Directory | [Boiling point ]
316.9±15.0 °C(Predicted) | [density ]
1.052 | [storage temp. ]
Inert atmosphere,Store in freezer, under -20°C | [pka]
10.23±0.10(Predicted) | [Appearance]
White to off-white Solid | [InChI]
InChI=1S/C11H21NO2S/c1-11(2,3)14-10(13)12-6-4-9(8-15)5-7-12/h9,15H,4-8H2,1-3H3 | [InChIKey]
VEPAXJUGIFPJNK-UHFFFAOYSA-N | [SMILES]
N1(C(OC(C)(C)C)=O)CCC(CS)CC1 |
| Hazard Information | Back Directory | [Synthesis]
A reaction was carried out with tert-butyl 4-((carbamoylimidothio)methyl)piperidine-1-carboxylate (1.2, 15 g, 1.00 eq., crude) as raw material with sodium hydroxide (2.2 g, 55.00 mmol, 1.00 eq.) in a mixture of methanol/water (1:2 v/v, 150 mL) under argon protection at 60 °C with stirring for 2 hours. After completion of the reaction, the reaction mixture was cooled to room temperature. The pH of the reaction solution was adjusted with 35% aqueous hydrochloric acid to 7. The reaction solution was extracted with ethyl acetate (3 x 50 mL) and the organic phases were combined. The organic phase was washed with saturated saline (2 x 50 mL), dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (eluent: ethyl acetate/petroleum ether=1:8 v/v) to give 5.6 g of yellow oily product in 44% yield. The structure of the product was confirmed by 1H-NMR (400 MHz, CDCl3): δ 4.13 (m, 2H), 2.69 (m, 2H), 2.46 (m, 2H), 1.82 (m, 2H), 1.50 (s, 9H), 1.32 (m, 1H), 1.18 (m, 2H) ppm. | [References]
[1] Patent: US2016/243100, 2016, A1. Location in patent: Paragraph 0078 |
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| Company Name: |
Cool Pharm, Ltd
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021-60455363 18019463053 |
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www.coolpharm.com |
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